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Chapter 22: Q72P-c (page 1205)

Show how you would use the malonic ester synthesis to make the following compounds

Short Answer

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Step1: Malonic ester synthesis

It鈥檚 a method in which a substituted derivative of acetic acid is formation occur in the presence of sodium ethoxide from dimethyl malonate followed by alkylation or acylation then hydrolysis followed by decarboxylation to form a derivate of acetic acid as a product.

Step by step solution

01

Step-by-Step Solution

Step1: Malonic ester synthesis

It鈥檚 a method in which a substituted derivative of acetic acid is formation occur in the presence of sodium ethoxide from dimethyl malonate followed by alkylation or acylation then hydrolysis followed by decarboxylation to form a derivate of acetic acid as a product.

02

Reaction followed by alkylation

Ethoxide is used as a base to form an enolate ion which on further reaction with the alkyl halide the alkylation that occur means the removal of the halide ion the alkyl group attached at the alpha position to the carbonyl.

03

Decarboxylation

It is the reaction that lead to the removal of the carbonyl group and releases carbon dioxideCO2. Decarboxylation occurs by providing heat in the reaction.

04

Mechanism

  1. Acidic hydrogen protonated
  2. Formation of enolate ion
  3. Alkylation
  4. Decarboxylation
  5. Derivative of acetic acid formed

Mechanism

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Question:Show how you would use an aldol, Claisen, or another type of condensation to make each compound

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